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9.1.1 Congenital glaucoma, Buphthalmos (96)
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61524 Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null MutationTuysuz B
JIMD reports 2015; 0:
61662 Optical Coherence Tomography in an Infant with Walker-Warburg SyndromeMano N
Case Reports in Ophthalmology 2015; 6: 210-215
61040 Neural crest derivatives in ocular development: Discerning the eye of the stormWilliams AL
Birth Defects Research Part C-Embryo Today: Reviews 2015; 105: 87-95
61310 Novel mutations in PAX6, OTX2 and NDP in anophthalmia, microphthalmia and colobomaDeml B
European Journal of Human Genetics 2016; 24: 535-541
61142 RETINAL AND CHOROIDAL CHANGES OF NANOPHTHALMIC EYES WITH AND WITHOUT SECONDARY GLAUCOMAXiao H
Retina (Philadelphia, Pa.) 2015; 35: 2121-2129
61379 Outcomes of Ahmed glaucoma valve implantation in advanced primary congenital glaucoma with previous surgical failureHuang J
Clinical Ophthalmology 2015; 9: 977-983
61308 Phakomatosis Pigmentovascularis Associated With Sturge-Weber Syndrome, Ota Nevus, and Congenital GlaucomaYang Y
Medicine 2015; 94: e1025
61560 Newborn Glaucoma with Imperforate PupilMandal AK
Optometry and Vision Science 2015; 92: e380-e382
60977 Polymorphic Variants of Cytochrome P450: Relevance to Cancer and Other DiseasesDaly AK
Advances in Pharmacology 2015; 74: 85-111
61522 Rare FOXC1 variants in congenital glaucoma: identification of translation regulatory sequencesMedina-Trillo C
European Journal of Human Genetics 2016; 24: 672-680
61537 Boston type 1 keratoprosthesis for primary congenital glaucomaHaugsdal JM
British Journal of Ophthalmology 2016; 100: 328-331
61550 PERIPHERAL RETINAL DEGENERATIONS AND RHEGMATOGENOUS DETACHMENT IN PRIMARY CONGENITAL GLAUCOMAGupta S
Retina (Philadelphia, Pa.) 2016; 36: 188-191
61125 Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and Brazilde Melo MB
PLoS ONE 2015; 10: e0127147
61341 A case of WAGR syndrome in association with developmental glaucoma requiring bilateral Baerveldt glaucoma implants and subsequent tube repositioningAkagi T
Clinical Ophthalmology 2015; 9: 1081-1084
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndromeZhu X
Gene 2015; 571: 142-144
61703 CYP1B1 gene analysis and phenotypic correlation in Portuguese children with primary congenital glaucomaCardoso MS
European Journal of Ophthalmology 2015; 0: 0
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucomaBashir R
Gene 2015; 570: 295-298
61550 PERIPHERAL RETINAL DEGENERATIONS AND RHEGMATOGENOUS DETACHMENT IN PRIMARY CONGENITAL GLAUCOMAGogia V
Retina (Philadelphia, Pa.) 2016; 36: 188-191
61379 Outcomes of Ahmed glaucoma valve implantation in advanced primary congenital glaucoma with previous surgical failureLin J
Clinical Ophthalmology 2015; 9: 977-983
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndromeDai FR
Gene 2015; 571: 142-144
61560 Newborn Glaucoma with Imperforate PupilRamappa M
Optometry and Vision Science 2015; 92: e380-e382
61537 Boston type 1 keratoprosthesis for primary congenital glaucomaGoins KM
British Journal of Ophthalmology 2016; 100: 328-331
61125 Genotype-Phenotype Correlations in CYP1B1-Associated Primary Congenital Glaucoma Patients Representing Two Large Cohorts from India and BrazilMandal AK
PLoS ONE 2015; 10: e0127147
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucomaTahir H
Gene 2015; 570: 295-298
61524 Phenotypic Expansion of Congenital Disorder of Glycosylation Due to SRD5A3 Null MutationPehlivan D
JIMD reports 2015; 0:
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